IrishJew wrote:
Thanks, guys! Perhaps a complete solution to this problem is up for the taking? I imagine it would involve the concept of tesselation. For example, 1,2 dichlorobenzene might have a higher boiling point than 1,4-dichlorobenzene because the molecules of the former tesselate better than the molecules of the latter. What do you think?
Believe it or not, I am extremely familiar with both of those chemicals lol, I have a ton of data on them (more than I ever wanted to have), I should have time to pull it up later tonight if you want. What's your interest? BTW, the boiling point difference is pretty small, about 5 degrees Celsius if my memory serves correctly, I'll look up the exact values later. They can be separated by distillation but crystallization is typically the better option, since their melting points are significantly different.